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抗菌药物与环糊精包合物:专利综述

Antibacterial drugs and cyclodextrin inclusion complexes: a patent review.

作者信息

Santos Anamaria Mendonça, Carvalho Santana Júnior Cláudio, Nascimento Júnior José Adão Carvalho, Andrade Tatianny de Araujo, Shanmugam Saravanan, Thangaraj Parimelazhagan, Frank Luiza Abrahão, Serafini Mairim Russo

机构信息

Postgraduate Program in Health Sciences, Federal University of Sergipe, Aracaju, Brazil.

Department of Pharmacy, Federal University of Sergipe, São Cristóvão, Brazil.

出版信息

Expert Opin Drug Deliv. 2023 Mar;20(3):349-366. doi: 10.1080/17425247.2023.2175815. Epub 2023 Feb 15.

Abstract

INTRODUCTION

Bacterial antibiotic resistance occurs when bacteria mutate and escape the effect of antibiotics, which makes the antibiotics no longer effective in treating infections. New solutions for bacterial infections are a persistent need including the identification of drugs with better pharmacological profiles, more potent, and safer. Cyclodextrins inclusion complexes have been able to improve the physicochemical and pharmacological properties of the formulation molecules, resulting in new alternatives with better efficacy.

AREAS COVERED

The patents analyzed in the review used treatments based on antibiotics already on the market, natural products, and synthesized molecules composed of the formulation with cyclodextrins. The combination between cyclodextrin and nanostructures also were presented in the patents review process. Moreover, inclusion complexes have been an alternative in developing treatment mainly in China by the pharmaceutical industries in several countries such as Germany, Hungary, the United States of America, Japan and China.

EXPERT OPINION

This review is broad and complete since it considers the first patent involving cyclodextrins and antibacterial drugs. Therefore, the various inclusion complexes and antibacterial drugs alternatives presented in this review offer therapeutic options to fight bacterial infections. If shown to be effective, these drugs may be extremely important in the current clinical practice.

摘要

引言

当细菌发生突变并逃避抗生素的作用时,就会出现细菌对抗生素的耐药性,这使得抗生素在治疗感染时不再有效。持续需要针对细菌感染的新解决方案,包括鉴定具有更好药理学特性、更有效且更安全的药物。环糊精包合物能够改善制剂分子的物理化学和药理学性质,从而产生具有更好疗效的新选择。

涵盖领域

本综述中分析的专利采用了基于市场上已有的抗生素、天然产物以及由环糊精制剂组成的合成分子的治疗方法。环糊精与纳米结构之间的组合也在专利审查过程中有所呈现。此外,包合物已成为德国、匈牙利、美国、日本和中国等多个国家的制药行业主要在中国开发治疗方法的一种选择。

专家意见

本综述广泛且全面,因为它考虑了涉及环糊精和抗菌药物的首个专利。因此,本综述中呈现的各种包合物和抗菌药物选择为对抗细菌感染提供了治疗选择。如果被证明有效,这些药物在当前临床实践中可能极其重要。

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